Allometric relationship between tissue respiration and body mass in a marine teleost, porgy Pagrus major

1993 ◽  
Vol 105 (1) ◽  
pp. 129-133 ◽  
Author(s):  
Oikawa Shin ◽  
Itazawa Yasuo
1997 ◽  
Vol 75 (3) ◽  
pp. 339-358 ◽  
Author(s):  
Jason F. Schreer ◽  
Kit M. Kovacs

Maximum diving depths and durations were examined in relation to body mass for birds, marine mammals, and marine turtles. There were strong allometric relationships between these parameters (log10 transformed) among air-breathing vertebrates (r = 0.71, n = 111 for depth; r = 0.84, n = 121 for duration), although there was considerable scatter around the regression lines. Many of the smaller taxonomic groups also had a strong allometric relationship between diving capacity (maximum depth and duration) and body mass. Notable exceptions were mysticete cetaceans and diving/flying birds, which displayed no relationship between maximum diving depth and body mass, and otariid seals, which showed no relationship between maximum diving depth or duration and body mass. Within the diving/flying bird group, only alcids showed a significant relationship (r = 0.81, n = 9 for depth). The diving capacities of penguins had the highest correlations with body mass (r = 0.81, n = 11 for depth; r = 0.93, n = 9 for duration), followed by those of odontocete cetaceans (r = 0.75, n = 21 for depth; r = 0.84, n = 22 for duration) and phocid seals (r = 0.70, n = 15 for depth; r = 0.59, n = 16 for duration). Mysticete cetaceans showed a strong relationship between maximum duration and body mass (r = 0.84, n = 9). Comparisons across the various groups indicated that alcids, penguins, and phocids are all exceptional divers relative to their masses and that mysticete cetaceans dive to shallower depths and for shorter periods than would be predicted from their size. Differences among groups, as well as the lack of relationships within some groups, could often be explained by factors such as the various ecological feeding niches these groups exploit, or by variations in the methods used to record their behavior.


2014 ◽  
Vol 84 (4) ◽  
pp. 1171-1178 ◽  
Author(s):  
J. Lucas ◽  
A. Schouman ◽  
L. Lyphout ◽  
X. Cousin ◽  
C. Lefrancois

2005 ◽  
Vol 15 (2) ◽  
pp. 65-71
Author(s):  
A.H. Clarke

The extensive remains of large sauropods, excavated in the Upper Jurassic layers of the Tendaguru region of Tanzania, East Africa by Janensch [15], include an intact fossil cast of a vestibular labyrinth and an endocast of the large Brachiosaurus brancai. The approximately 150 million year old labyrinth cast demonstrates clearly a form and organisation congruent in detail to those of extant vertebrate species. Besides the near-orthogonal arrangement of semicircular canals (SCCs), the superior and inferior branches of the vestibulo-acoustic nerve, the endolymphatic duct, the oval and round windows, and the cochlea can be identified. The orientation of the labyrinth in the temporal bone is also equivalent to that of many extant vertebrates. Furthermore, the existence of the twelve cranial nerves can be identified from the endocast. The present study was initiated after the photogrammetric measurement of the skeleton volume of B. brancai [13] yielded a realistic estimate of body mass (74.42 metric tons). Dimensional analysis shows that body mass and average SCC dimensions of B. brancai generally fit with the allometric relationship found in previous studies of extant species. However, the anterior SCC is significantly larger than the allometric relationship would predict. This would indicate greater sensitivity, supporting the idea that the behavioural repertoire must have included much slower pitch movements of the head. These slower movements would most likely have involved flexion of the neck, rather than head pitching about the atlas joint. Pursuing the relationship between body mass and SCC dimensions further, the SCC frequency response is estimated by scaling up from the SCC dimensions of the rhesus monkey; this yields a range between 0.008–26 Hz, approximately one octave lower than for humans.


Author(s):  
Koichiro Gen ◽  
Sonoko Yamaguchi ◽  
Koichi Okuzawa ◽  
Hirohiko Kagawa ◽  
Md. Samsul Alam

1988 ◽  
Vol 255 (5) ◽  
pp. R760-R767 ◽  
Author(s):  
C. A. Beuchat ◽  
E. J. Braun

In reptiles, there are two pairs of kidneys at birth: the mesonephros and the metanephros. The metanephric kidney in reptiles, as in all amniote vertebrates, is retained as the functional kidney in adults. However, the reptilian mesonephros does not degenerate until after birth, and its function during this time is unknown. In neonates of the iguanid lizard Sceloporus jarrovi, the metanephric kidney is only 63% as large as predicted from the allometric relationship between kidney mass and body mass in adults. However, the kidney mass of neonatal lizards conforms to this prediction if the mesonephric and metanephric masses are combined. Some other amniote vertebrates appear to follow this pattern as well: in marsupials, which retain the mesonephros for a short period after birth, the sum of mesonephric and metanephric mass in neonates conforms to the allometry of kidney mass on body mass for adults. In contrast, the mesonephros of eutherian mammals is degenerate at birth and the metanephric kidney alone is of the predicted size. That the scaling of kidney mass in neonatal lizards and marsupials is the same as that of adults only if the mass of both the mesonephros and metanephros are combined suggests that the mesonephric kidney in these vertebrates plays a significant role in the regulation of water and ion balance during development and for at least a short time after birth.


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